The Most Frequently Preferred Surgical Method In The Treatment Of Sacrococcygeal Pilonidal Disease

January 5, 2021 updated by: Alpaslan Şahin, Konya Meram State Hospital

The Most Frequently Preferred Surgical Method In The Treatment Of Sacrococcygeal Pilonidal Disease; Multicenter Cohort Study

There is no consensus on which procedure is the ideal surgical method in the treatment of sacrococcygeal pilonidal disease (SPD). The study aimed to retrospectively screen the cases that had undergone surgical treatment for SPD in the last 15 years in four different tertiary Stage hospitals and analyze the most frequently used surgical treatment method and its results.

Study Overview

Status

Completed

Conditions

Detailed Description

The researchers in our study will retrospectively scan the records of patients who have been operated on for SPD in the last 15 years at Health Sciences University Konya Health Practice and Research Center, Selçuk University Medical Faculty Hospital, Necmettin Erbakan University Medical Faculty Hospital, and Başkent University Medical Faculty Hospital General Surgery Clinics.

Demographic characteristics of the patients, type of anesthesia, duration of operation, duration of hospitalization, time to return to work or school, final healing time, follow-up time, and recurrence information will be transferred to the SPSS statistics program analyzed.

The researchers could not find any articles in the literature on the subject. Therefore, this study will contribute to the literature.

Study Type

Observational

Enrollment (Actual)

6748

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Turkey
      • Konya, Turkey, 42090
        • Konya Training and Research Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

14 years to 80 years (Child, Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

All patients aged 14-80 years who underwent surgery for pilonidal sinus constitute the study population.

Description

Inclusion Criteria:

  • All patients between the ages of 14-80 who underwent surgery for pilonidal sinus

Exclusion Criteria:

  • unregulated diabetes mellitus
  • collagen tissue disease
  • decompensated cardiovascular disease
  • cases with missing follow-up information

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Cohort
  • Time Perspectives: Retrospective

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Type of surgery method
Time Frame: 15 day
The ratio of each type of surgery to the study population
15 day
duration of surgery
Time Frame: 15 day
The average operation time of the determined types of surgery will be determined.
15 day
hospitalization time
Time Frame: 15 day
The average hospitalization time of the determined types of surgery will be determined.
15 day
Type of anesthesia
Time Frame: 15 day
the ratio of anesthesia methods to the study population
15 day
day time return to work
Time Frame: 15 days
return to work time will be found as average days for specified surgery types.
15 days
complete healing time
Time Frame: 15 days
Complete healing time will be found as average days for specified surgery types
15 days
recurrence
Time Frame: 15 days
recurrence rate in the study population
15 days

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Konya Meram State Hospital

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

October 22, 2020

Primary Completion (Actual)

November 25, 2020

Study Completion (Actual)

December 15, 2020

Study Registration Dates

First Submitted

October 18, 2020

First Submitted That Met QC Criteria

October 18, 2020

First Posted (Actual)

October 22, 2020

Study Record Updates

Last Update Posted (Actual)

January 6, 2021

Last Update Submitted That Met QC Criteria

January 5, 2021

Last Verified

January 1, 2021

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • HSU Konya HPRC General Surgery

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

IPD Plan Description

No plans to make individual participant data (IPD) available to other researchers

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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